Sociodemographic Disparities in Postoperative Nausea and Vomiting von Lee, Donaldson C., Vetter, Thomas R., Dobyns, Jeffrey B., Crump, Sandra J., Benz, David L., Short, Roland T., Parks, Dale A., Beasley, T. Mark, Liwo, Amandiy N.

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Preoperative Risk Stratification: Identifying Modifiable Risks for Optimization von Sherrer, Matthew, Simmons, Jeffrey W., Dobyns, Jeffrey B.

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The Early History of Laryngology von Mandabach, Mark G., Dobyns, Jeffrey B.

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PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia von Jansen, Laura A, Mirzaa, Ghayda M, Ishak, Gisele E, O'Roak, Brian J, Hiatt, Joseph B, Roden, William H, Gunter, Sonya A, Christian, Susan L, Collins, Sarah, Adams, Carissa, Rivière, Jean-Baptiste, St-Onge, Judith, Ojemann, Jeffrey G, Shendure, Jay, Hevner, Robert F, Dobyns, William B

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Therapeutic Hypothermia after In-Hospital Cardiac Arrest in Children von Moler, Frank W, Silverstein, Faye S, Holubkov, Richard, Slomine, Beth S, Christensen, James R, Nadkarni, Vinay M, Meert, Kathleen L, Browning, Brittan, Pemberton, Victoria L, Page, Kent, Gildea, Marianne R, Scholefield, Barnaby R, Shankaran, Seetha, Hutchison, Jamie S, Berger, John T, Ofori-Amanfo, George, Newth, Christopher J.L, Topjian, Alexis, Bennett, Kimberly S, Koch, Joshua D, Pham, Nga, Chanani, Nikhil K, Pineda, Jose A, Harrison, Rick, Dalton, Heidi J, Alten, Jeffrey, Schleien, Charles L, Goodman, Denise M, Zimmerman, Jerry J, Bhalala, Utpal S, Schwarz, Adam J, Porter, Melissa B, Shah, Samir, Fink, Ericka L, McQuillen, Patrick, Wu, Theodore, Skellett, Sophie, Thomas, Neal J, Nowak, Jeffrey E, Baines, Paul B, Pappachan, John, Mathur, Mudit, Lloyd, Eric, van der Jagt, Elise W, Dobyns, Emily L, Meyer, Michael T, Sanders, Ronald C, Clark, Amy E, Dean, J. Michael

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Semiquantitative analysis of hypothalamic damage on MRI predicts risk for hypothalamic obesity von Roth, Christian L., Eslamy, Hedieh, Werny, David, Elfers, Clinton, Shaffer, Michele L., Pihoker, Catherine, Ojemann, Jeffrey, Dobyns, William B.

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Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder von Christian, Susan L, Brune, Camille W, Sudi, Jyotsna, Kumar, Ravinesh A, Liu, Shaung, Karamohamed, Samer, Badner, Judith A, Matsui, Seiichi, Conroy, Jeffrey, McQuaid, Devin, Gergel, James, Hatchwell, Eli, Gilliam, T. Conrad, Gershon, Elliot S, Nowak, Norma J, Dobyns, William B, Cook, Edwin H

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Diffusion Tensor Imaging in Boys With Adrenoleukodystrophy: Identification of Cerebral Disease and Association With Neurocognitive Outcomes von Pierpont, Elizabeth I, Labounek, René, Gupta, Ashish, Lund, Troy, Orchard, Paul J, Dobyns, William B, Bondy, Monica, Paulson, Amy, Metz, Andrew, Shanley, Ryan, Wozniak, Jeffrey R, Mueller, Bryon A, Loes, Daniel, Nascene, David, Nestrasil, Igor

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Genotypically Defined Lissencephalies Show Distinct Pathologies von Forman, Mark S, Squier, Waney, Dobyns, William B, Golden, Jeffrey A

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Polymicrogyria Includes Fusion of the Molecular Layer and Decreased Neuronal Populations But Normal Cortical Laminar Organization von Judkins, Alexander R, Martinez, Daniel, Ferreira, Pamela, Dobyns, William B, Golden, Jeffrey A

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Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care von Pirozzi, Filomena, Berkseth, Matthew, Shear, Rylee, Gonzalez, Lorenzo, Timms, Andrew E, Sulc, Josef, Pao, Emily, Oyama, Nora, Forzano, Francesca, Conti, Valerio, Guerrini, Renzo, Doherty, Emily S, Saitta, Sulagna C, Lockwood, Christina M, Pritchard, Colin C, Dobyns, William B, Novotny, Edward, Wright, Jason N N, Saneto, Russell P, Friedman, Seth, Hauptman, Jason, Ojemann, Jeffrey, Kapur, Raj P, Mirzaa, Ghayda M

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Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum von Chizhikov, Victor V, Uyanik, Gökhan, Kuechler, Alma, Kutsche, Kerstin, Flubacher, Armin, Charnas, Lawrence R, Golden, Jeffrey A, Haas, Carola A, Frank, Ulrich, Ullmann, Reinhard, Klopocki, Eva, Dobyns, William B, Sudi, Jyotsna, Wimplinger, Isabella, Christian, Susan L, Horn, Denise, Najm, Juliane

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Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism von Mirzaa, Ghayda M, Campbell, Catarina D, Solovieff, Nadia, Goold, Carleton P, Jansen, Laura A, Menon, Suchithra, Timms, Andrew E, Conti, Valerio, Biag, Jonathan D, Olds, Carissa, Boyle, Evan August, Collins, Sarah, Ishak, Gisele, Poliachik, Sandra L, Girisha, Katta M, Yeung, Kit-San, Chung, Brian Hon Yin, Rahikkala, Elisa, Gunter, Sonya A, McDaniel, Sharon S, Macmurdo, Colleen Forsyth, Bernstein, Jonathan A, Martin, Beth, Leary, Rebecca J, Mahan, Scott, Liu, Shanming, Weaver, Molly, Dorschner, Michael O, Jhangiani, Shalini, Muzny, Donna M, Boerwinkle, Eric, Gibbs, Richard A, Lupski, James R, Shendure, Jay, Saneto, Russell P, Novotny, Edward J, Wilson, Christopher J, Sellers, William R, Morrissey, Michael P, Hevner, Robert F, Ojemann, Jeffrey G, Guerrini, Renzo, Murphy, Leon O, Winckler, Wendy, Dobyns, William B

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Wide spectrum of developmental brain disorders from megalencephaly to focal cortical dysplasia and pigmentary mosaicism caused by mutations of MTOR von Mirzaa, Ghayda M., Campbell, Catarina D., Solovieff, Nadia, Goold, Carleton, Jansen, Laura A., Menon, Suchithra, Timms, Andrew E., Conti, Valerio, Biag, Jonathan D., Adams, Carissa, Boyle, Evan August, Collins, Sarah, Ishak, Gisele, Poliachik, Sandra, Girisha, Katta M., Yeung, Kit San, Chung, Brian Hon Yin, Rahikkala, Elisa, Gunter, Sonya A., McDaniel, Sharon S., Macmurdo, Colleen Forsyth, Bernstein, Jonathan A., Martin, Beth, Leary, Rebecca, Mahan, Scott, Liu, Shanming, Weaver, Molly, Doerschner, Michael, Jhangiani, Shalini, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Lupski, James R., Shendure, Jay, Saneto, Russell P., Novotny, Edward J., Wilson, Christopher J., Sellers, William R., Morrissey, Michael, Hevner, Robert F., Ojemann, Jeffrey G., Guerrini, Renzo, Murphy, Leon O., Winckler, Wendy, Dobyns, William B.

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Pathological subtypes of polymicrogyria and brain development von Judkins, Alexander Russell, Dobyns, William B., Golden, Jeffrey A.

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Pathological subtypes of polymicrogyria and brain development: 127.4 von Judkins, Alexander Russell, Dobyns, William B., Golden, Jeffrey A.

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Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal von Keegan, Catherine E., Vilain, Eric, Mohammed, Mansoor, Lehoczky, Jessica, Dobyns, William B., Archer, Steven M., Innis, Jeffrey W.

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Linkage of a Human Brain Malformation, Familial Holoprosencephaly, to Chromosome 7 and Evidence for Genetic Heterogeneity von Muenke, Maximilian, Gurrieri, Fiorella, Bay, Carolyn, Yi, David H., Collins, Amanda L., Johnson, Virginia P., Raoul C. M. Hennekam, Schaefer, G. Bradley, Weik, LuAnn, Lubinsky, Mark S., Daack-Hirsch, Sandy, Moore, Cynthia A., Dobyns, William B., Murray, Jeffrey C., Price, R. Arlen

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Erratum: Corrigendum: Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum von Najm, Juliane, Horn, Denise, Wimplinger, Isabella, Golden, Jeffrey A, Chizhikov, Victor V, Sudi, Jyotsna, Christian, Susan L, Ullmann, Reinhard, Kuechler, Alma, Haas, Carola A, Flubacher, Armin, Charnas, Lawrence R, Uyanik, Gökhan, Frank, Ulrich, Klopocki, Eva, Dobyns, William B, Kutsche, Kerstin

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Correction: Corrigendum: Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum von Najm, Juliane, Horn, Denise, Wimplinger, Isabella, Golden, Jeffrey A, Chizhikov, Victor V, Sudi, Jyotsna, Christian, Susan L, Ullmann, Reinhard, Kuechler, Alma, Haas, Carola A, Flubacher, Armin, Charnas, Lawrence R, Uyanik, Gökhan, Frank, Ulrich, Klopocki, Eva, Dobyns, William B, Kutsche, Kerstin

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